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MAGEL2
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Most Correlated Tissues
Pituitary gland
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Superior cervical ganglion
Atrioventricular node
Granulocyte-macrophage progenitor cell of bone marrow
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Clinical characteristics and genetic analysis of a case of infantile Schaaf-Yang syndrome due to a h…
Cellular and disease functions of the Prader-Willi Syndrome gene MAGEL2.
Dopamine pathway imbalance in mice lacking Magel2, a Prader-Willi syndrome candidate gene.
Progressive postnatal decline in leptin sensitivity of arcuate hypothalamic neurons in the Magel2-nu…
Truncating Mutations of MAGEL2, a Gene within the Prader-Willi Locus, Are Responsible for Severe Art…
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Evaluation of Tolerance, Suckling and Food Intake After Repeated Nasals Administrations of Oxytocin …
Tolerance of Intranasal Administration of OT in Prader-Willi Newborn Babies
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